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[ CAS No. 189281-66-1 ] {[proInfo.proName]}

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Chemical Structure| 189281-66-1
Chemical Structure| 189281-66-1
Structure of 189281-66-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 189281-66-1 ]

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Product Details of [ 189281-66-1 ]

CAS No. :189281-66-1 MDL No. :MFCD02180634
Formula : C7H4Cl2FNO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :WADLLLSMEPLCNO-UHFFFAOYSA-N
M.W : 224.02 Pubchem ID :2775354
Synonyms :

Calculated chemistry of [ 189281-66-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.49
TPSA : 39.19 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.73 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.02
Log Po/w (XLOGP3) : 2.73
Log Po/w (WLOGP) : 2.73
Log Po/w (MLOGP) : 1.94
Log Po/w (SILICOS-IT) : 2.94
Consensus Log Po/w : 2.47

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.16
Solubility : 0.156 mg/ml ; 0.000694 mol/l
Class : Soluble
Log S (Ali) : -3.21
Solubility : 0.139 mg/ml ; 0.000621 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.62
Solubility : 0.0537 mg/ml ; 0.00024 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.98

Safety of [ 189281-66-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 189281-66-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 189281-66-1 ]

[ 189281-66-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 189281-66-1 ]
  • [ 124-41-4 ]
  • [ 959616-64-9 ]
YieldReaction ConditionsOperation in experiment
97% In methanol; at 20℃; for 1h; [00670] Intermediate 73b: methyl 2-chloro-5-fluoro-6-methoxy-pyridine-3-carboxylate[00671] Sodium methoxide (1 .86mL, 11.91 mmol) was added to methyl 2,6-dichloro-5-fluoro-pyridine-3-carboxylate (1 .8g, 8.O3mmol) in Methanol (9mL) and the resultant mixture was left to stir for 1 hour. To the mixture was added EtOAc (20 mL) and water (20 mL), the layers were separated and the organ ics extracted using EtOAc (3 x 20 mL). Organic fractions were collected, dried (Na2SO4), filtered and reduced in vacuo to afford the desired product methyl 2-chloro-5-fluoro-6- methoxy-pyridine-3-carboxylate (1 .72g, 7.83mmol, 97% yield) as an orange solid.1H NMR (CDCI3,400MHZ) Olppm: 7.92 (1H, d, J= 9.6 Hz), 4.09 (3H, 5), 3.92 (3H, 5). MS Method 2: RT: 1.71 mm, 220.0 mlz [M+H]
With methanol; at 20℃; for 0.666667h; To a solution of 1.5 g of methyl 2,6-dichloro-5-fluoronicotinate in 12 mL of methanol, a solution of 1.3 g of 28% sodium methoxide/methanol in 3 mL of methanol was dropped, and the mixture was stirred at room temperature for 40 minutes. Thereto were added water and ethyl acetate, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 1.2 g of methyl 2-chloro-5-fluoro-6-methoxynicotinate as a white solid. 1H-NMR (CDCl3) delta: 3.92 (3H, s), 4.09 (3H, s), 7.92 (1H, d, J = 9.8 Hz)
  • 3
  • [ 189281-66-1 ]
  • [ 886372-63-0 ]
  • 4
  • [ 189281-66-1 ]
  • [ 884494-73-9 ]
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